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Results: 1-7 |
Results: 7
Response of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndrome
Authors: Paavonen, KJ Swan, H Piippo, K Hokkanen, L Laitinen, P Viitasalo, M Toivonen, L Kontula, K
Citation: Kj. Paavonen et al., Response of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndrome, HEART, 86(1), 2001, pp. 39-44
A founder mutation of the potassium channel KCNQ1 in long QT syndrome - Implications for estimation of disease prevalence and molecular diagnostics
Authors: Piippo, K Swan, H Pasternack, M Chapman, H Paavonen, K Viitasalo, M Toivonen, L Kontula, K
Citation: K. Piippo et al., A founder mutation of the potassium channel KCNQ1 in long QT syndrome - Implications for estimation of disease prevalence and molecular diagnostics, J AM COL C, 37(2), 2001, pp. 562-568
Effect of the antimalarial drug Halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A
Authors: Piippo, K Holmstrom, S Swan, H Viitasalo, M Raatikka, M Toivonen, L Kontula, K
Citation: K. Piippo et al., Effect of the antimalarial drug Halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A, AM J CARD, 87(7), 2001, pp. 909
Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns
Authors: Piippo, K Laitinen, P Swan, H Toivonen, L Viitasalo, M Pasternack, M Paavonen, K Chapman, H Wann, KT Hirvela, E Sajantila, A Kontula, K
Citation: K. Piippo et al., Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns, J AM COL C, 35(7), 2000, pp. 1919-1925
Neuroleptanesthesia: current status
Authors: Bissonnette, B Swan, H Ravussin, P Un, V
Citation: B. Bissonnette et al., Neuroleptanesthesia: current status, CAN J ANAES, 46(2), 1999, pp. 154-168
Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
Authors: Swan, H Piippo, K Viitasalo, M Heikkila, P Paavonen, T Kainulainen, K Kere, J Keto, P Kontula, I Toivonen, L
Citation: H. Swan et al., Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts, J AM COL C, 34(7), 1999, pp. 2035-2042
Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects
Authors: Swan, H Viitasalo, M Piippo, K Laitinen, P Kontula, K Toivonen, L
Citation: H. Swan et al., Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects, J AM COL C, 34(3), 1999, pp. 823-829
Risultati: 1-7 |